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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Beverages

Lipton Diet Green Tea Citrus Recalled for Undeclared Aspartame

Agency Publication Date: July 18, 2023
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Summary

Pepsico Inc has voluntarily recalled approximately 300 24-packs of Lipton Diet Green Tea Citrus. The recall was initiated because the 16.9 fl. oz. bottles contain undeclared aspartame and lack the mandatory "Phenylketonurics: Contains Phenylalanine" warning required for products containing this sweetener. No incidents or injuries have been reported to date.

Risk

Aspartame contains phenylalanine, which poses a serious health risk to individuals with phenylketonuria (PKU), a rare genetic disorder that prevents the body from properly processing that amino acid.

What You Should Do

  1. This recall affects Lipton Diet Green Tea Citrus sold in 24-packs of 16.9 fl. oz. bottles with UPC 0-12000-01722-3.
  2. Check your product for code SEP172023XXXXAG06133 and a Best By date of SEP 17 2023, which are the specific identifiers for the affected units.
  3. Return the product to the place of purchase for a refund, throw it away, or contact Pepsico Inc for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Lipton Diet Green Tea Citrus (24 pack of 16.9 fl. oz. bottles)
UPC Codes:
012000017223
Lot Numbers:
SEP172023XXXXAG06133 (Best By SEP 17 2023)

Recall #: F-1286-2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92683
Status: Resolved
Manufacturer: Pepsico Inc
Manufactured In: United States
Units Affected: 300, 24 packs (retail unit)
Distributed To: Indiana, Tennessee, Ohio, Kentucky

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.